Variant (rsID / SNP)
rs292557
rs292557 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR91. Location: chromosome 7, position 134,871,775. The table records no clinical significance for this variant.
Reference-table entries
WDR91Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:134871775
- HGVS
- NM_001362737.2,c.2106G>A,p.Ser702Ser
- Allele change
- Silent
Associated conditions / phenotypes
Synonymous_S695S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.